跳至主要内容
临床试验/CTRI/2022/05/042810
CTRI/2022/05/042810已完成4 期

A prospective, post market, non-interventional observational, open label, single arm, single center study to confirm clinical safety and performance of SkanRespiro Plus and Pranaa

Skanray Technologies Limited0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • Adult and pediatric subjects of age more than two year or body weight of 10 kg above whichever is lower and of either gender.
  • Subjects who need mechanical ventilation.
  • Subject or the legally authorised representative on behalf of subject shall be capable of understanding and signing the informed consent form.

排除标准

  • Subjects with age less than two year or less than 10 kg of body weight.
  • Subjects who need ventilation during transport.
  • Pregnant or nursing mother.
  • Unconscious subjects shall be excluded from the non invasive mode of ventilation.

研究者

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